54178-94-8

Basic information

• Product Name: 4-[[(3-Aminophenyl)sulfonyl]amino]-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-2-naphthalenecarboxamide
• Synonyms: 4-[[(3-Aminophenyl)sulfonyl]amino]-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-2-naphthalenecarboxamide
• CAS NO: 54178-94-8
• Molecular Formula: C37H47N3O5S
• Molecular Weight: 645.8512
• Mol File: 54178-94-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.2g/cm³
• Refractive Index: 1.609
• PKA: 7.90±0.50(Predicted)
• CAS DataBase Reference: 4-[[(3-Aminophenyl)sulfonyl]amino]-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-2-naphthalenecarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[[(3-Aminophenyl)sulfonyl]amino]-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-2-naphthalenecarboxamide(54178-94-8)
• EPA Substance Registry System: 4-[[(3-Aminophenyl)sulfonyl]amino]-N-[4-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyl]-1-hydroxy-2-naphthalenecarboxamide(54178-94-8)

Safety Data

• Hazardous Substances Data: 54178-94-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C37H47N3O5S/c1-7-36(3,4)25-18-19-33(31(22-25)37(5,6)8-2)45-21-12-11-20-39-35(42)30-24-32(28-16-9-10-17-29(28)34(30)41)40-46(43,44)27-15-13-14-26(38)23-27/h9-10,13-19,22-24,40-41H,7-8,11-12,20-21,38H2,1-6H3,(H,39,42)

Downstream Products

• 54241-47-3 C₄₇H₅₂N₄O₇S 
• 54179-42-9 4-[3-(4,8-Dihydroxy-naphthalen-1-ylazo)-benzenesulfonylamino]-1-hydroxy-naphthalene-2-carboxylic acid {4-[2,4-bis-(1,1-dimethyl-propyl)-phenoxy]-butyl}-amide 

Relevant articles and documents

Yellow azopyrazoline dye releasing redox compounds for photographic color transfer

A photosensitive element comprising a support having thereon at least one photosensitive silver halide emulsion layer and one of said layers having associated therewith a yellow image dye-releasing compound having a formula as follows STR1 wherein Car represents a sulfonamidophenol or sulfonamidonaphthol carrier moiety which, as a function of oxidation under alkaline conditions, releases a diffusible dye from said compound. X represents a bivalent linking group of the formula --R1 --Ln --R1p -- where each R1 can be the same or different and each represents alkylene phenylene; or substituted phenylene; L represents a bivalent radical selected from oxy, carbonyl, carboxamido, carbamoyl, sulfonamido, sulfamoyl, sulfinyl or sulfonyl; n is an integer having a value of 0 or 1; p is 1 when n equals 1 and p is 1 or 0 when n equals 0, provided that when p is 1 the carbon content of the sum of both R radicals does not exceed 14 carbon atoms; R represents hydrogen or alkyl; J represents a bivalent radical selected from sulfonyl or carbonyl; m and q each represent an integer having a value of 0 or 1; E represents hydrogen, halogen, alkyl or alkoxy; Z represents hydrogen or an electron withdrawing group selected from cyano, trifluoromethyl, alkylsulfonyl, substituted alkylsulfonyl, phenylsulfonyl, or substituted phenylsulfonyl; a carboxylic acid ester having the formula --COOR2 wherein R2 is alkyl, phenyl or substituted phenyl; sulfo, a sulfamoyl radical having the formula --SO2 NR3 R4 wherein R3 represents hydrogen or alkyl, and R4 represents hydrogen, alkyl, substituted alkyl; benzyl, phenyl, substituted phenyl; alkylcarbonyl, or phenylcarbonyl, with the proviso that the carbon content of the sum of R3 and R4 not exceed 14 carbon atoms; a carbamoyl radical having the formula --CON(R3)2 wherein each R3 can be the same or different and is as described previously; and M represents hydrogen, a solubilizing group or precursor thereof selected from carboxy, sulfo, a sulfamoyl radical as described for Z or a carboxylic acid ester as described for Z.